Cargando…
Animal Models of Ehlers–Danlos Syndromes: Phenotype, Pathogenesis, and Translational Potential
The Ehlers–Danlos syndromes (EDS) are a group of heritable connective tissues disorders mainly characterized by skin hyperextensibility, joint hypermobility and generalized tissue fragility. Currently, 14 EDS subtypes each with particular phenotypic features are recognized and are caused by genetic...
Autores principales: | Vroman, Robin, Malfait, Anne-Marie, Miller, Rachel E., Malfait, Fransiska, Syx, Delfien |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8547655/ https://www.ncbi.nlm.nih.gov/pubmed/34712265 http://dx.doi.org/10.3389/fgene.2021.726474 |
Ejemplares similares
-
The Ehlers–Danlos Syndromes against the Backdrop of Inborn Errors of Metabolism
por: Van Damme, Tim, et al.
Publicado: (2022) -
Sensory profiling in classical Ehlers-Danlos syndrome: a case-control study revealing pain characteristics, somatosensory changes, and impaired pain modulation
por: Colman, Marlies, et al.
Publicado: (2023) -
Ehlers-Danlos Syndrome, Hypermobility Type, Is Linked to Chromosome 8p22-8p21.1 in an Extended Belgian Family
por: Syx, Delfien, et al.
Publicado: (2015) -
Glycosaminoglycan linkage region of urinary bikunin as a potentially useful biomarker for β3GalT6‐deficient spondylodysplastic Ehlers–Danlos syndrome
por: Nikpour, Mahnaz, et al.
Publicado: (2022) -
Vascular phenotypes in nonvascular subtypes of the Ehlers-Danlos syndrome: a systematic review
por: D'hondt, Sanne, et al.
Publicado: (2018)